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Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant
  1. Dr J R Vermeesch, Center for Human Genetics, Herestraat 49, 3000 Leuven, Belgium; joris.vermeesch{at}uz.kuleuven.ac.be
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Hannes FD, Sharp AJ, Mefford HC, et al
Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant

Publication history

  • Received 5 October 2007
  • Revised 28 December 2007
  • Accepted 7 January 2008
  • Published in print 1 April 2009.
  • Published online 8 April 2009.
  • Published first 11 June 2008.

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